Peliosis hepatis: 2 case reports of a rare liver disorder and its differential diagnosis

Medicine (Baltimore). 2017 Mar;96(13):e6471. doi: 10.1097/MD.0000000000006471.

Abstract

Rationale: Peliosis hepatis (PH) is a rare tumor-like liver lesion composed of multiple blood-filled cavities within the liver parenchyma. It is hard to differentiate PH from other liver lesions by imaging, such as carcinoma, metastases, or abscess.

Patient concerns: Here, we reported 2 cases that presented with liver lesions under ultrasound and computed tomography (CT) scanning, without any history of liver diseases or drug usage traced back.

Diagnoses: Liver biopsy and laparoscopy were processed, and the lesions were eventually diagnosed as PH by histopathology, which microscopically presented with multiple sinusoidal dilatations with blood-filled cystic spaces.

Interventions: After the liver biopsy or laparoscopy, the patients were discharged and followed up in the clinic.

Outcomes: Both patients were followed up for at least 1 year with good recovery.

Lessons: PH should always be recognized in the differentiation of liver lesions, particularly indistinctive lesion(s) without any history of liver-related diseases.

Publication types

  • Case Reports

MeSH terms

  • Diagnosis, Differential
  • Female
  • Humans
  • Liver / pathology
  • Male
  • Middle Aged
  • Peliosis Hepatis / diagnostic imaging*
  • Peliosis Hepatis / pathology